Job Description

• Define and edit mock tables, listings and figures (TLFs) and analysis dataset specifications.
• Generate, document, and maintain analysis datasets.
• Develop scripts for wrangling / data transformation and standardizing assay datasets.
• Create ad hoc, standard and study-specific reports (e.g. SMC, DSMB, SMB, Assay QC); may perform cross-study reporting.
• Test and de-bug programs and maintain version control on production programs and scripts.
• Design and develop new work instructions (WIs) and updates to existing WIs.
• Work with clinical programmers, lab programmers, statisticians, and other statistical programmers to resolve data quality, processing, and analysis issues.
• Contribute to mentoring and training of junior Statistical Programmers and may supervise as neede

• Bachelor's degree in computer science or a scientific, technical, or health-related field.
• t least five years of experience in R programming, with additional experience in other programming languages, experience using version control tools (e.g. git or svn).
• t least four years of experience in support of clinical trials, in clinical research setting or other health research setting, or in data wrangling/transformation within a health-related field.
• Demonstrated ability to communicate effectively in a matrix management environment as a member of several project teams.
• Knowledge of and experience with clinical trials research data.
• Graduate degree in computer science or a scientific, technical, or health-related field.
• 3+years of statistical programming in clinical research setting or R programming in a health-related field.

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